One of the most intriguing questions about electron transfer proteins is how the protein modifies the electron transfer properties of its redox site. This knowledge is crucial in understanding the molecular basis of metabolic processes, diseases involving these processes, and drug design targeting these processes. The overall goal is to understand the properties of electron transfer proteins at a molecular level. The focus is on the iron-sulfur proteins, which are ubiquitous proteins involved in pathways as respiration, photosynthesis, and biosynthesis. Key issues we address are the stabilization by the protein of [4Fe-4S]3+/2+ in HiPIPs, [4Fe-4S]2+/1+ in ferredoxins, and [4Fe-4S]1+/0 in nitrogenase Fe-protein in aim 1, the intramolecular transfer in the "wire" of seven [4Fe-4S] clusters found in respiratory complex I in aim 2, and the Fe-S cluster assembly pathway in aim 3. Our approach uses continuum electrostatic calculations, molecular dynamics simulations, electronic structure calculations, and sequence and structural bioinformatics. An overriding aim in this period is to develop simple models that describe the architecture of metalloproteins with a few essential parameters based on our accumulated experience with these proteins. The models will be used to develop simple, fast software tools for predicting redox properties and metal binding sites of metalloproteins. In addition, these architectural models will be used in developing process models for protein-mediated electron transfer, which are essential for theoretical studies of large systems such as the respiratory complex I. Features of these models will be tested using other calculation techniques and experimental results from our collaborators. Moreover, these models will provide a framework for designing new calculations and experiments.
The specific aims are:
Aim 1. Develop an architectural model for reduction potentials of metalloproteins Aim 2. Develop models for protein-mediated electron transfer Aim 3. Develop models for conversion of Fe-S clusters in proteins

Public Health Relevance

Computational studies of electron transfer proteins provide a fundamental, molecular understanding of the metabolic processes that move energy around living cells such as respiration and photosynthesis. This knowledge is crucial in understanding diseases that involve these processes and designing drugs to target these diseases. For instance, dysfunction in respiratory complex I has been associated with human neurodegenerative diseases and aging.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM045303-21
Application #
8204420
Study Section
Macromolecular Structure and Function A Study Section (MSFA)
Program Officer
Preusch, Peter C
Project Start
1992-02-01
Project End
2013-11-30
Budget Start
2011-12-01
Budget End
2012-11-30
Support Year
21
Fiscal Year
2012
Total Cost
$298,078
Indirect Cost
$98,987
Name
Georgetown University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Perrin Jr, B Scott; Ichiye, Toshiko (2013) Identifying residues that cause pH-dependent reduction potentials. Biochemistry 52:3022-4
Perrin Jr, Bradley Scott; Niu, Shuqiang; Ichiye, Toshiko (2013) Calculating standard reduction potentials of [4Fe-4S] proteins. J Comput Chem 34:576-82
Perrin Jr, Bradley Scott; Ichiye, Toshiko (2013) Characterizing the effects of the protein environment on the reduction potentials of metalloproteins. J Biol Inorg Chem 18:103-10
Perrin Jr, Bradley Scott; Ichiye, Toshiko (2013) Identifying sequence determinants of reduction potentials of metalloproteins. J Biol Inorg Chem 18:599-608
Mitra, Devrani; Pelmenschikov, Vladimir; Guo, Yisong et al. (2011) Dynamics of the [4Fe-4S] cluster in Pyrococcus furiosus D14C ferredoxin via nuclear resonance vibrational and resonance Raman spectroscopies, force field simulations, and density functional theory calculations. Biochemistry 50:5220-35
Luo, Yan; Ergenekan, Can E; Fischer, Justin T et al. (2010) The molecular determinants of the increased reduction potential of the rubredoxin domain of rubrerythrin relative to rubredoxin. Biophys J 98:560-8
Perrin Jr, Bradley Scott; Ichiye, Toshiko (2010) Fold versus sequence effects on the driving force for protein-mediated electron transfer. Proteins 78:2798-808
Niu, Shuqiang; Ichiye, Toshiko (2009) Insight into environmental effects on bonding and redox properties of [4Fe-4S] clusters in proteins. J Am Chem Soc 131:5724-5
Niu, Shuqiang; Ichiye, Toshiko (2009) Probing ligand effects on the redox energies of [4Fe-4S] clusters using broken-symmetry density functional theory. J Phys Chem A 113:5671-6
Niu, Shuqiang; Ichiye, Toshiko (2009) Cleavage of [4Fe-4S]-type clusters: breaking the symmetry. J Phys Chem A 113:5710-7

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